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局限性硬皮病与系统性红斑狼疮并存:两例报告

Concurrent linear scleroderma and systemic lupus erythematosus: a report of two cases.

作者信息

Mackel S E, Kozin F, Ryan L M, Sheth K J, Jordon R E

出版信息

J Invest Dermatol. 1979 Nov;73(5):368-72. doi: 10.1111/1523-1747.ep12550429.

Abstract

Two patients with linear scleroderma (en coup de sabre) developed systemic lupus erythematosus (SLE). This association has been well documented in only one previous case. The presence of high titer antibodies to ribonucleoprotein (RNP) initially led to the diagnosis of the mixed connective tissue disease. Development of more serious clinical involvement and antibodies to Sm (case 1) or native deoxyribonucleic acid (nDNA) (case 2) helped establish a diagnosis of SLE. Use of these studies in the differential diagnosis of systemic rheumatic diseases is disucssed briefly. The presence of anti-RNAP antibodies in patients with localized scleroderma may herald a more serious rheumatic disease.

摘要

两名患有线性硬皮病(剑伤样硬皮病)的患者出现了系统性红斑狼疮(SLE)。这种关联仅在之前的一例病例中有充分记录。最初,高滴度核糖核蛋白(RNP)抗体的存在导致了混合性结缔组织病的诊断。更严重的临床症状以及针对Sm(病例1)或天然脱氧核糖核酸(nDNA)(病例2)抗体的出现,有助于确立SLE的诊断。本文简要讨论了这些研究在系统性风湿性疾病鉴别诊断中的应用。局限性硬皮病患者中抗RNAP抗体的存在可能预示着更严重的风湿性疾病。

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